https://scholars.lib.ntu.edu.tw/handle/123456789/564126
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Hsu C.-C. | en_US |
dc.contributor.author | Chuang W.-J. | en_US |
dc.contributor.author | Chang C.-H. | en_US |
dc.contributor.author | Tseng Y.-L. | en_US |
dc.contributor.author | Peng H.-C. | en_US |
dc.contributor.author | TUR-FU HUANG | en_US |
dc.date.accessioned | 2021-05-31T07:03:18Z | - |
dc.date.available | 2021-05-31T07:03:18Z | - |
dc.date.issued | 2011 | - |
dc.identifier.issn | 15387933 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/564126 | - |
dc.description.abstract | Background and objectives:Septic shock is a major cause of morbidity and mortality in intensive care units, but there is still no effective therapy for the patients. We evaluated the effects of rhodostomin (Rn), an Arg-Gly-Asp-containing snake venom disintegrin, on lipopolysaccharide (LPS)-activated phagocytes in vitro and LPS-induced endotoxemia in vivo. Methods and results:Rn inhibited adhesion, migration, cytokine production and mitogen-activated protein kinase (MAPK) activation of macrophage induced by LPS. Flow cytometric analysis revealed that Rn specifically blocked anti-αv mAb binding to RAW264.7. Besides inhibiting MAPK activation of THP-1, Rn bound to LPS-activated THP-1 and specifically blocked anti-αvβ3 mAb binding to THP-1. Binding assays proved that integrin αvβ3 was the binding site for rhodostomin on phagocytes. Rn reversed the enhancement of fibronectin and vitronectin on LPS-induced monocyte adhesion and cytokine release. Transfection of integrin αv siRNA also inhibited LPS-induced activation of monocyte, and Rn exerted no further inhibitory effect. Furthermore, Rn significantly decreased the production of tumor necrosis factor-α (TNF-a), interleukin (IL)-6, -1β and -10 and attenuated cardiovascular dysfunction, including blood pressure and heart pulse, and thrombocytopenia in LPS-induced endotoxemic mice. Rn also protected against tissue inflammation as evidenced by histological examination. Conclusions:Rn may interact with αvβ3 integrin of monocytes/macrophages leading to interfere with the activation of phagocytes triggered by LPS. These results suggest that the protective function of Rn in LPS-induced endotoxemia may be attributed to its anti-inflammation activities in vivo. ? 2011 International Society on Thrombosis and Haemostasis. | - |
dc.relation.ispartof | Journal of Thrombosis and Haemostasis | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | cytokine; disintegrin; fibronectin; interleukin 10; interleukin 1beta; interleukin 6; lipopolysaccharide; mitogen activated protein kinase; rhodostomin; small interfering RNA; tumor necrosis factor alpha; unclassified drug; vitronectin; vitronectin receptor; animal cell; animal experiment; animal model; animal tissue; antiinflammatory activity; article; binding site; blood pressure; cardiovascular disease; cell adhesion; cell migration; cytokine production; cytokine release; drug effect; endotoxemia; enzyme activation; heart rate; histopathology; human; human cell; immunohistochemistry; in vitro study; macrophage; male; mortality; mouse; nonhuman; phagocyte; priority journal; signal transduction; thrombocytopenia; tissue injury; Animals; Binding Sites; Cell Adhesion; Cell Line; Cell Movement; Cytokines; Disintegrins; Endotoxemia; Humans; Integrin alphaVbeta3; Lipopolysaccharides; Macrophage Activation; Male; MAP Kinase Signaling System; Mice; Mice, Inbred ICR; Peptides; Phagocytes; RNA Interference; RNA, Small Interfering; Thrombocytopenia | - |
dc.title | Improvements in endotoxemic syndromes using a disintegrin, rhodostomin, through integrin alphav beta 3-dependent pathway | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1111/j.1538-7836.2010.04163.x | - |
dc.identifier.pmid | 21143376 | - |
dc.identifier.scopus | 2-s2.0-79952062165 | - |
dc.relation.pages | 593-602 | - |
dc.relation.journalvolume | 9 | - |
dc.relation.journalissue | 3 | - |
item.cerifentitytype | Publications | - |
item.fulltext | no fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.openairetype | journal article | - |
item.grantfulltext | none | - |
crisitem.author.dept | Pharmacology | - |
crisitem.author.orcid | 0000-0001-9252-938X | - |
crisitem.author.parentorg | College of Medicine | - |
顯示於: | 藥理學科所 |
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